1918 Results for "

1a

" in MedChemExpress (MCE) Product Catalog:
Products (1918)

1918 Results for "1a" in MCE Product Catalog:

153
153 Publications Verification
Cat. No.: HY-50202
CAS No.: 124083-20-1
Synonyms: (R)-(+)-Etomoxir
Etomoxir ((R)-(+)-Etomoxir) is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig.
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153
153 Publications Verification
Cat. No.: HY-50202A
CAS No.: 828934-41-4
Synonyms: (R)-(+)-Etomoxir sodium salt
Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig [1].
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31
31 Cited Publications
Cat. No.: HY-15602
CAS No.: 1256388-51-8
Purity:  99.69%
Synonyms: GS-5885
Target:  

HCV SARS-CoV

Research Areas:  

Infection

Ledipasvir (GS-5885) is an inhibitor of the hepatitis C virus NS5A, with EC50s of 34 pM and 4 pM against genotype 1a and 1b replicon, respectively. Ledipasvir is also a SARS-CoV 3CL pro inhibitor with an IC50 of 1.62 μM .
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27
27 Cited Publications
Cat. No.: HY-P7018
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IGF1; Somatomedin-C; Insulin Like Growth Factor 1; IGF1a; IGF-I; MGF; Insulin-Like Growth Factor 1; Insulin-Like Growth Factor IB; Insulin-Like Growth Factor I; Insulin-Like Growth Factor-I; IGFI; Alternative Protein IGF1; IGF; Somatomedin C; Insulin-Like
Species:  
Human
Source:  
E. coli
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20
20 Cited Publications
Cat. No.: HY-10238
CAS No.: 850876-88-9
Purity:  99.67%
Synonyms: ITMN-191; R7227; RO5190591; RG7227
Target:  

HCV Protease HCV SARS-CoV

Research Areas:  

Infection

Danoprevir (ITMN-191) is an orally active NS3/4A protease inhibitor for hepatitis C virus (HCV) with an IC50 of 0.29 nM and is selective for NS3/4A over a panel of 53 proteases (IC50 higher than 10 μM). Danoprevir (ITMN-191) inhibits HCV genotypes 1a, 1b, 4, 5, and 6 (IC50s=0.2-0.4 nM) as well as 2b and 3a (IC50s=1.6, 3.5 nM) [1] . Danoprevir is also a SARS-CoV 3CL pro inhibitor with an IC50 of 0.05 μM .
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15
15 Cited Publications
Cat. No.: HY-13998
CAS No.: 1132935-63-7
Purity:  98.17%
Synonyms: ABT-333
Target:  

HCV DNA/RNA Synthesis

Research Areas:  

Infection

Dasabuvir (ABT-333) is a nonnucleoside hepatitis C virus (HCV) polymerase inhibitor. Dasabuvir inhibits RNA-dependent RNA polymerase encoded by the HCV NS5B gene. Dasabuvir inhibits genotype 1a (strain H77) and 1b (strain Con1) replicons, with EC50 values of 7.7 and 1.8 nM, respectively [1].
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15
15 Cited Publications
Cat. No.: HY-10349A
CAS No.: 1092679-51-0
Purity:  99.77%
Research Areas:  

Neurological Disease

WAY-100635 maleate is a potent and selective 5-hydroxytryptamine 1A (5-HT1A) receptor antagonist with an IC50 value of 0.91 nM and Ki value of 0.39 nM. WAY-100635 maleate has pIC50 values for 5-HT1A and α1-adrenergic receptors of 8.9 and 6.6, respectively. WAY-100635 maleate is also a potent dopamine D4 receptor agonist [1] .
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15
15 Cited Publications
Cat. No.: HY-10349
CAS No.: 162760-96-5
Purity:  99.51%
Research Areas:  

Neurological Disease

WAY-100635 is a potent and selective 5-HT1A Receptor antagonist with a pIC50 of 8.87, an apparent pA2 of 9.71. WAY-100635 is a potent and selective 5-hydroxytryptamine 1A (5-HT1A) receptor antagonist with an IC50 value of 0.91 nM and Ki value of 0.39 nM. WAY-100635 has pIC50 values for 5-HT1A and α1-adrenergic receptors of 8.9 and 6.6, respectively. WAY-100635 is also a potent dopamine D4 receptor agonist [1] .
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13
13 Cited Publications
Cat. No.: HY-12594
CAS No.: 1216941-48-8
Purity:  99.87%
Synonyms: ABT-450; Veruprevir
Target:  

HCV Protease HCV SARS-CoV

Research Areas:  

Infection

Paritaprevir (ABT-450) is a potent, orally active and antiviral non-structural protein 3/4A (NS3/4A) protease inhibitor with EC50s of 1 and 0.21 nM against HCV 1a and 1b, respectively. Paritaprevir is also a SARS-CoV 3CL pro inhibitor with an IC50 of 1.31 μM. Paritaprevir is metabolized primarily by cytochrome P450 (CYP) 3A. The plasma concentration and half-life of Paritaprevir can be enhanced by Ritonavir (a CYP450 inhibitor) [1] .
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13
13 Cited Publications
Cat. No.: HY-P7051A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NOG; Symphalangism 1 (Proximal); Prev. SYNS1; SYNS1a; Prev. SYM1; Noggin; Synostoses (Multiple) Syndrome 1
Species:  
Human
Source:  
CHO
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13
13 Cited Publications
Cat. No.: HY-P7086
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NOG; Symphalangism 1 (Proximal); Prev. SYNS1; SYNS1a; Prev. SYM1; Noggin; Synostoses (Multiple) Syndrome 1
Species:  
Mouse
Source:  
CHO
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12
12 Cited Publications
Cat. No.: HY-P7070
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: IGF1; Somatomedin-C; Insulin Like Growth Factor 1; IGF1a; IGF-I; MGF; Insulin-Like Growth Factor 1; Insulin-Like Growth Factor IB; Insulin-Like Growth Factor I; Insulin-Like Growth Factor-I; IGFI; Alternative Protein IGF1; IGF; Somatomedin C; Insulin-Like
Species:  
Mouse
Source:  
E. coli
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11
11 Cited Publications
Cat. No.: HY-15789
CAS No.: 1370468-36-2
Purity:  99.97%
Synonyms: MK-8742
Target:  

HCV

Research Areas:  

Infection

Elbasvir (MK-8742) is a hepatitis C virus nonstructural protein 5A (HCV NS5A) inhibitor with EC50s of 4, 3 and 3 nM against genotype 1a, 1b, and 2a, respectively.
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10
10 Cited Publications
Cat. No.: HY-P80438
Synonyms: A26C1a antibody; A26C1B antibody; ACTB antibody; ACTB_HUMAN antibody; Actin beta antibody; Actin cytoplasmic 1 antibody; Actin, cytoplasmic 1, N-terminally processed antibody; Actx antibody; b actin antibody; Beta cytoskeletal actin antibody; Beta-actin antibody; BRWS1 antibody; E430023M04Rik antibody; MGC128179 antibody; PS1TP5 binding protein 1 antibody; PS1TP5BP1 antibody; β-actin antibody

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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9
9 Cited Publications
Cat. No.: HY-104064
CAS No.: 1430208-73-3
Purity:  99.72%
Target:  

Ras Apoptosis

Research Areas:  

Cancer

1A-116, a potent Rac1 inhibitor, is specific for W56 residues, can prevent EGF-induced Rac1 activation and block Rac1-P-Rex1 interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a concentration-dependent manner. 1A-116 also demonstrates a high antimetastatic activity in vivo [1] .
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9
9 Cited Publications
Cat. No.: HY-P70558
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NOG; Symphalangism 1 (Proximal); Prev. SYNS1; SYNS1a; Prev. SYM1; Noggin; Synostoses (Multiple) Syndrome 1
Species:  
Human
Source:  
HEK293
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9
9 Cited Publications
Cat. No.: HY-P80704
Synonyms: HIF1a; BHLHE78; MOP1; PASD8; Hypoxia-inducible factor 1-alpha; HIF-1-alpha; HIF1-alpha; ARNT-interacting protein; Basic-helix-loop-helix-PAS protein MOP1; Class E basic helix-loop-helix protein 78; bHLHe78; Member of PAS protein 1; PAS doma

Host:  

Rabbit

Application:  

WB, ICC/IF, ELISA

Reactivity:  

Human, Mouse, Rat

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8
8 Cited Publications
Cat. No.: HY-12782T
CAS No.: 1431303-72-8
Purity:  99.98%
Synonyms: ORY-1001 dihydrochloride; RG6016 dihydrochloride; RO 7051790 dihydrochloride
Target:  

Histone Demethylase

Research Areas:  

Cancer

Iadademstat (ORY-1001) dihydrochloride is a selective irreversible lysine (K)-specific demethylase 1A (KDM1A/LSD1) inhibitor.
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8
8 Cited Publications
Cat. No.: HY-12294A
Purity:  ≥98.0%
Synonyms: NVP-AAM077 tetrasodium hydrate
Target:  

Apoptosis Caspase iGluR

Research Areas:  

Neurological Disease

PEAQX tetrasodium hydrate (NVP-AAM077 tetrasodium hydrate) is a tetrasodium hydrate of PEAQX (HY-12294). PEAQX tetrasodium hydrate is an orally active and selective NMDA antagonist, with IC50 values of 270 nM and 29.6 μM for hNMDAR 1A/2A and hNMDAR 1A/2B, respectively. PEAQX tetrasodium hydrate can promote the activation of caspase-3 and induce cell apoptosis in cortical striatal slice cultures [1] .
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7
7 Cited Publications
Cat. No.: HY-P1411
CAS No.: 880107-52-8
Synonyms: PcTx1; Psalmopoeus cambridgei toxin-1
Research Areas:  

Neurological Disease Cancer

Psalmotoxin 1 (PcTx1) is a protein toxin that can bind at subunit-subunit interfaces of acid-sensing ion channel 1a (ASIC1a). Psalmotoxin 1 is a potent and slective ASIC1a inhibitor (IC50: 0.9 nM) by increasing the apparent affinity for H + of ASIC1a. Psalmotoxin 1 can induce cell apoptosis, also inhibits cell migration, proferliration and invasion of cancer cells. Psalmotoxin 1 can be used in the research of cancers, or neurological disease [1] .
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